Canonical Allele Identifier: CA2650970348

Gene: AGT

Linked Data

• gnomAD v4: 1-230702393-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230702393C>A , CM000663.2:g.230702393C>A	GRCh38
NC_000001.10:g.230838139C>A , CM000663.1:g.230838139C>A	GRCh37
NC_000001.9:g.228904762C>A	NCBI36
NG_008836.1:g.17198G>T
NG_008836.2:g.17198G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679738.1:c.*748G>T	ENSP00000505063.1:n.*748G>T
ENST00000679802.1:c.*1638G>T	ENSP00000505184.1:n.*1638G>T
ENST00000679854.1:n.6484G>T
ENST00000680041.1:c.*748G>T	ENSP00000504866.1:n.*748G>T
ENST00000680783.1:c.829+7602G>T	ENSP00000506329.1:n.829+7602G>T
ENST00000681347.1:n.4285G>T
ENST00000681514.1:c.*748G>T	ENSP00000505963.1:n.*748G>T
ENST00000681772.1:c.*1673G>T	ENSP00000505829.1:n.*1673G>T